G79R (p.Gly79Arg) variant of KRT3 (Keratin, type II cytoskeletal 3)
G79R (p.Gly79Arg) in KRT3 (Keratin, type II cytoskeletal 3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data and structural context.
G79R (p.Gly79Arg) variant details
- p.Gly79Arg
- gnomAD rs1400103770
- Missense
- Variant Prioritization Score for Impact Estimate 0.47
- REVEL 0.50
- CADD 17.20
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available